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FDA 510(k)

STAYFREE DEODORANT MINI-PADS

K-Number: K760853 · 1976-11-11

Decision Date1976-11-11
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

STAYFREE DEODORANT MINI-PADS is the device name listed in this FDA 510(k) record. The listed applicant is Personal Products Co.. It received FDA 510(k) clearance on 1976-11-11 under 510(k) number K760853. The device is classified under product code HHL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAYFREE DEODORANT MINI-PADS?

STAYFREE DEODORANT MINI-PADS is a medical device that received FDA 510(k) clearance on 1976-11-11. The listed applicant is Personal Products Co.. The 510(k) number is K760853.

When did STAYFREE DEODORANT MINI-PADS receive FDA 510(k) clearance?

STAYFREE DEODORANT MINI-PADS received FDA 510(k) clearance on 1976-11-11, under 510(k) number K760853.

Who is the listed applicant for STAYFREE DEODORANT MINI-PADS?

The FDA 510(k) record lists Personal Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STAYFREE DEODORANT MINI-PADS?

The FDA product code for STAYFREE DEODORANT MINI-PADS is HHL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Personal Products Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 45 devices →

Related Devices (Code: HHL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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